Evidence map›Paper›PMID 36450726›Full record

ArticleNature communications2022

Analysis of the first genetic engineering attribution challenge.

Oliver M Crook, Kelsey Lane Warmbrod, Greg Lipstein, Christine Chung, Christopher W Bakerlee, T Greg McKelvey, Shelly R Holland, Jacob L Swett, Kevin M Esvelt, Ethan C Alley and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Synsor: a tool for alignment-free detection of engineered DNA sequences.Frontiers in bioengineering and biotechnology · 2024
    Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Oliver M CrookOxford Protein Informatics Group, Department of Statistics, University of Oxford, Oxford, UK.ORCID 0000-0001-5669-8506
Kelsey Lane WarmbrodJohns Hopkins Center for Health Security, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.ORCID 0000-0003-4326-7541
Greg LipsteinDrivenData Inc, Denver, CO, USA.
Christine ChungDrivenData Inc, Denver, CO, USA.
Christopher W BakerleealtLabs Inc, Berkeley, CA, USA.
T Greg McKelveyaltLabs Inc, Berkeley, CA, USA.ORCID 0000-0001-8552-3385
Shelly R HollandaltLabs Inc, Berkeley, CA, USA.
Jacob L SwettaltLabs Inc, Berkeley, CA, USA.
Kevin M EsveltaltLabs Inc, Berkeley, CA, USA.
Ethan C AlleyaltLabs Inc, Berkeley, CA, USA. ethan@altlabs.tech.ORCID 0000-0002-8219-7382
William J BradshawaltLabs Inc, Berkeley, CA, USA. wjbrad@mit.edu.ORCID 0000-0002-7345-3866
Altlabs · USJohns Hopkins University · USOxford Research Group · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability to identify the designer of engineered biological sequences-termed genetic engineering attribution (GEA)-would help ensure due credit for biotechnological innovation, while holding designers accountable to the communities they affect. Here, we present the results of the first Genetic Engineering Attribution Challenge, a public data-science competition to advance GEA techniques. Top-scoring teams dramatically outperformed previous models at identifying the true lab-of-origin of engineered plasmid sequences, including an increase in top-1 and top-10 accuracy of 10 percentage points. A simple ensemble of prizewinning models further increased performance. New metrics, designed to assess a model's ability to confidently exclude candidate labs, also showed major improvements, especially for the ensemble. Most winning teams adopted CNN-based machine-learning approaches; however, one team achieved very high accuracy with an extremely fast neural-network-free approach. Future work, including future competitions, should further explore a wide diversity of approaches for bringing GEA technology into practical use.

Indexed as

BiotechnologyGenetic EngineeringCloning, MolecularGenetic TechniquesSocial Perception

Identifiers

PMID36450726
PMCPMC9712580
OpenAlexW3206890433

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.